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FDA 510(k)

ANGIOGRAPHY NEEDLE W/WO CONNECTION

K-Number: K840923 · 1984-04-17

ApplicantDlp, Inc.
Decision Date1984-04-17
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANGIOGRAPHY NEEDLE W/WO CONNECTION is the device name listed in this FDA 510(k) record. The listed applicant is Dlp, Inc.. It received FDA 510(k) clearance on 1984-04-17 under 510(k) number K840923. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIOGRAPHY NEEDLE W/WO CONNECTION?

ANGIOGRAPHY NEEDLE W/WO CONNECTION is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Dlp, Inc.. The 510(k) number is K840923.

When did ANGIOGRAPHY NEEDLE W/WO CONNECTION receive FDA 510(k) clearance?

ANGIOGRAPHY NEEDLE W/WO CONNECTION received FDA 510(k) clearance on 1984-04-17, under 510(k) number K840923.

Who is the listed applicant for ANGIOGRAPHY NEEDLE W/WO CONNECTION?

The FDA 510(k) record lists Dlp, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANGIOGRAPHY NEEDLE W/WO CONNECTION?

The FDA product code for ANGIOGRAPHY NEEDLE W/WO CONNECTION is DYB.

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Related Devices (Code: DYB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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